2795-76-8 Usage
Description
(4-Chlorophenyl)(4-fluorophenyl)Methanol, also known as 4-(4-chlorophenyl)-4-(4-fluorophenyl)butan-1-ol, is an organic compound that features a methanol molecule with chlorophenyl and fluorophenyl groups attached. (4-Chlorophenyl)(4-fluorophenyl)Methanol is recognized for its potential applications in the pharmaceutical industry and organic chemistry.
Uses
Used in Pharmaceutical Research:
(4-Chlorophenyl)(4-fluorophenyl)Methanol is used as a potential intermediate in the synthesis of various medications. Its unique structure allows for the creation of diverse pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Organic Chemistry:
(4-Chlorophenyl)(4-fluorophenyl)Methanol serves as a building block in the production of other organic compounds. Its chlorophenyl and fluorophenyl groups provide a foundation for further chemical reactions and the synthesis of more complex molecules.
Used in Pharmacological Studies:
(4-Chlorophenyl)(4-fluorophenyl)Methanol is also studied for its potential pharmacological properties. Researchers are interested in understanding how this compound interacts with biological systems and whether it can be used to develop new treatments for various medical conditions.
Safety Precautions:
It is important to handle (4-Chlorophenyl)(4-fluorophenyl)Methanol with care due to its potential risks and hazards. As with all chemicals, it should be used according to safety guidelines and procedures to ensure the safety of both the users and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 2795-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,9 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2795-76:
(6*2)+(5*7)+(4*9)+(3*5)+(2*7)+(1*6)=118
118 % 10 = 8
So 2795-76-8 is a valid CAS Registry Number.
2795-76-8Relevant articles and documents
[Ir(COD)Cl]2/tris(2,4-di-t-butylphenyl)phosphite-catalyzed addition reactions of arylboronic acids with aldehydes
Liao, Yuan-Xi,Dong, Jie,Hu, Qiao-Sheng
supporting information, p. 1548 - 1550 (2018/03/26)
[Ir(COD)Cl]2/tris(2,4-di-t-butylphenyl)phosphite-catalyzed addition reactions of arylboronic acids with aldehydes were described. The Ir(I) catalyst, generated from [Ir(COD)Cl]2 and tris(2,4-di-t-butylphenyl)phosphite, was an efficient catalyst system for the addition reactions of a variety of arylboronic acids with aromatic and aliphatic aldehydes. The easy availability of the catalyst and good yields make these reactions potentially useful in organic synthesis.
CuCl/bipyridine-catalyzed addition reactions of arylboroxines with aldehydes, α,β-unsaturated ketones, and N-tosyl aldimines
Liao, Yuan-Xi,Hu, Qiao-Sheng
experimental part, p. 7602 - 7607 (2011/11/12)
CuCl/bipyridine-catalyzed addition reactions of arylboroxines with aldehydes and α,β-unsaturated ketones at elevated temperatures were described. By using the microwave energy, CuCl/bipyridine-catalyzed addition reactions of arylboroxines with aldimines were also realized.
Carbinol derivatives via rhodium-catalyzed addition of potassium trifluoro(organo)borates to aldehydes
Pucheault, Mathieu,Darses, Sylvain,Genet, Jean-Pierre
, p. 4714 - 4716 (2007/10/03)
Reaction of potassium aryltrifluoroborates with aldehydes, in the presence of a rhodium catalyst, afforded carbinol derivatives in high yields under mild aqueous conditions; this efficient reaction proved to be general, allowing the production of highly hindered diarylmethanols and aliphatic aldehydes were also reactive under these conditions. The Royal Society of Chemistry 2005.
